TY - JOUR
T1 - Production of murine collagen-induced arthritis using Klebsiella pneumoniae O3 lipopolysaccharide as a potent immunological adjuvant
AU - Takahashi, Kazuko
AU - Kato, Yutaka
AU - Sugiyama, Tsuyoshi
AU - Koide, Naoki
AU - Kawai, Makoto
AU - Fukada, Masako
AU - Yoshida, Tomoaki
AU - Yokochi, Takashi
PY - 1999
Y1 - 1999
N2 - Collagen-induced arthritis (CIA) was produced in mice with non H-2(q) and H-2(r) haplotypes by repeated immunization of porcine type-II collagen (CH) together with Klebsiella O3 lipopolysaccharide (KO3 LPS) as an immunological adjuvant. Histological changes that appeared in joints of repeatedly immunized mice were characterized by destruction of normal joint structure, synovial hyperplasia with proliferation of synovial cells, and infiltration of inflammatory cells. No such lesions were produced in mice receiving repeated injections of CII alone or KO3 LPS alone. Development of the humoral antibody and the delayed-type hypersensitivity to CH was exclusively found in mice immunized with the mixture of CII and KO3 LPS. It was therefore suggested that arthritis lesions induced by repeated immunization with the mixture of CII and KO3 LPS might be caused by an autoimmune mechanism, and that the experimental model might be useful for characterization of human rheumatoid arthritis (RA).
AB - Collagen-induced arthritis (CIA) was produced in mice with non H-2(q) and H-2(r) haplotypes by repeated immunization of porcine type-II collagen (CH) together with Klebsiella O3 lipopolysaccharide (KO3 LPS) as an immunological adjuvant. Histological changes that appeared in joints of repeatedly immunized mice were characterized by destruction of normal joint structure, synovial hyperplasia with proliferation of synovial cells, and infiltration of inflammatory cells. No such lesions were produced in mice receiving repeated injections of CII alone or KO3 LPS alone. Development of the humoral antibody and the delayed-type hypersensitivity to CH was exclusively found in mice immunized with the mixture of CII and KO3 LPS. It was therefore suggested that arthritis lesions induced by repeated immunization with the mixture of CII and KO3 LPS might be caused by an autoimmune mechanism, and that the experimental model might be useful for characterization of human rheumatoid arthritis (RA).
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U2 - 10.1111/j.1348-0421.1999.tb02472.x
DO - 10.1111/j.1348-0421.1999.tb02472.x
M3 - Article
C2 - 10524798
AN - SCOPUS:0032800579
SN - 0385-5600
VL - 43
SP - 795
EP - 801
JO - MICROBIOLOGY and IMMUNOLOGY
JF - MICROBIOLOGY and IMMUNOLOGY
IS - 8
ER -